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Extended Producer Responsibility as a Medical Device Manufacturer in the LUCID Packaging Register – Sustainability Starts with circular packaging design

Vanguard AG is often viewed solely as a service provider in the field of medical device reprocessing. However, our responsibilities extend far beyond that. As a manufacturer of CE-certified reprocessed medical devices, we hold the same obligations as any other manufacturer bringing products to market. This status carries with it a particular responsibility, not only for our medical devices but also for their packaging. Additionally, we place significant importance on sustainability and actively contribute to global environmental protection. Through our participation in the LUCID Packaging Register and our partnership with Cleanhub, we take responsibility for the environmentally sound disposal and recycling of packaging – whether for CS or CE-certified reprocessed medical devices.
14. August 2024
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Why the LUCID Packaging Register Is Important

The Packaging Act (VerpackG) requires all companies that place packaged products on the market in Germany to register with the LUCID Verpackungsregister of the Central Packaging Register Office (ZSVR). The aim of this legislation is to increase recycling rates and thereby protect the environment. All packaging that ends up as waste with the end consumer must be licensed and properly disposed of.

Our Dual Responsibility as a Medical Device Manufacturer

At Vanguard AG, we fulfill our obligations related to the LUCID Packaging Register for the packaging of our products, regardless of the type of reprocessing—whether CS or CE-certified. Our responsibilities include:

  • Official Registration: As both a manufacturer and distributor, we are required to register with the LUCID Packaging Register for all packaged products we bring to market. This registration ensures that we meet our obligations for the proper disposal and recycling of packaging.
  • System Participation Obligation: For each piece of packaging we place on the market, we participate in a dual system for the collection, sorting, and recycling of packaging materials.
  • Reporting and Proof of Quantity: We are obligated to report the quantities of packaging we place on the market to the ZSVR and provide proof of our participation in the dual system. This is a key step in ensuring that we minimize our ecological footprint.

Vanguard AG: Focus on Sustainability and Responsibility

In addition to fulfilling our obligations under the LUCID Packaging Register, we have partnered with Cleanhub, which collects non-recyclable plastic at different locations worldwide where there is a lack of effective recycling technologies. Cleanhub repurposes this plastic to create new products or uses it for energy generation in the respective regions. Through this partnership, we actively support the collection and recycling of plastic on a international scale, contributing to the reduction of global plastic pollution.

Conclusion

Vanguard AG is more than just a service provider! We are a full-fledged medical device re-manufacturer, bringing reprocessed CE-certified medical devices to market alongside our reprocessing services. Our commitments under the LUCID Packaging Register reflect our dedication to minimizing our ecological footprint and fulfilling our responsibilities as a manufacturer. Whether it’s CS or CE-certified products, we take these duties seriously and actively contribute to protecting the environment. By embracing our dual responsibilities—both as medical device manufacturers and stewards of sustainable packaging practices—we reinforce our commitment to environmental stewardship.

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